US20050029917A1 - Magnetron - Google Patents

Magnetron Download PDF

Info

Publication number
US20050029917A1
US20050029917A1 US10/912,099 US91209904A US2005029917A1 US 20050029917 A1 US20050029917 A1 US 20050029917A1 US 91209904 A US91209904 A US 91209904A US 2005029917 A1 US2005029917 A1 US 2005029917A1
Authority
US
United States
Prior art keywords
cathode
magnetron
fibers
electron emission
graphite nano
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US10/912,099
Other versions
US7474042B2 (en
Inventor
Masayuki Aiga
Toshiyuki Tsukada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Assigned to MATSUSHITA ELECTRIC INDUSTRIAL CO. LTD. reassignment MATSUSHITA ELECTRIC INDUSTRIAL CO. LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AIGA, MASAYUKI, TSUKADA, TOSHIYUKI
Publication of US20050029917A1 publication Critical patent/US20050029917A1/en
Assigned to PANASONIC CORPORATION reassignment PANASONIC CORPORATION CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD.
Application granted granted Critical
Publication of US7474042B2 publication Critical patent/US7474042B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J23/00Details of transit-time tubes of the types covered by group H01J25/00
    • H01J23/02Electrodes; Magnetic control means; Screens
    • H01J23/04Cathodes
    • H01J23/05Cathodes having a cylindrical emissive surface, e.g. cathodes for magnetrons
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y10/00Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J25/00Transit-time tubes, e.g. klystrons, travelling-wave tubes, magnetrons
    • H01J25/50Magnetrons, i.e. tubes with a magnet system producing an H-field crossing the E-field
    • H01J25/52Magnetrons, i.e. tubes with a magnet system producing an H-field crossing the E-field with an electron space having a shape that does not prevent any electron from moving completely around the cathode or guide electrode
    • H01J25/58Magnetrons, i.e. tubes with a magnet system producing an H-field crossing the E-field with an electron space having a shape that does not prevent any electron from moving completely around the cathode or guide electrode having a number of resonators; having a composite resonator, e.g. a helix
    • H01J25/587Multi-cavity magnetrons
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2201/00Electrodes common to discharge tubes
    • H01J2201/30Cold cathodes
    • H01J2201/304Field emission cathodes
    • H01J2201/30446Field emission cathodes characterised by the emitter material
    • H01J2201/30453Carbon types
    • H01J2201/30461Graphite
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2201/00Electrodes common to discharge tubes
    • H01J2201/30Cold cathodes
    • H01J2201/304Field emission cathodes
    • H01J2201/30446Field emission cathodes characterised by the emitter material
    • H01J2201/30453Carbon types
    • H01J2201/30469Carbon nanotubes (CNTs)

Definitions

  • the present invention relates to a field emission type magnetron used for a high frequency heating device such as a microwave range or a pulse generator such as a radar.
  • thermo-electron emission In a usual thermo-electron emission type magnetron, a hot cathode is used as an electron source.
  • the hot cathode supplies electrons by emitting thermo-electrons.
  • a thermo-electron emission is a mechanism that free electrons of a conduction band of the cathode obtain thermal energy by heating a material at about 1500 to 2700 K so that the free electrons get over a surface potential barrier to be emitted to a space.
  • FIG. 6 is a longitudinally sectional view showing one example of a usual thermo-electron emission type magnetron.
  • a hot cathode 2 is disposed at a central part of a plurality of anode vanes 1 .
  • the hot cathode 2 is formed in such a manner that tungsten wire rods 3 including thorium are formed helically at substantially equal intervals and both end parts are held by end hat parts 4 . Electric current is supplied to the hot cathode 2 to raise the temperature of the cathode to about 2000K and emit thermo-electrons (for instance, see JP-A-2001-23531).
  • a field emission type magnetron provided with a cathode that employs a usual field emission phenomenon uses a metallic foil as an electrode, as well known (for instance, see Japanese Patent No.2740793).
  • the field emission phenomenon means a phenomenon that a high electric field (about 10 9 V/m) is applied to a part near the surface of a material to allow the potential barrier on the surface of the material to be thin and electrons to be emitted outside the material without getting over the potential barrier due to a tunnel effect generated by the surge characteristics of the electrons.
  • a high electric field about 10 9 V/m
  • the field intensity of the surface of the cathode is 10 7 V/m.
  • an electrode for a field emission needs to have a structure that a radius of curvature of an end is small like a needle or a foil and improve a field concentration effect.
  • FIG. 7 is a longitudinally sectional view showing the structure of main parts of the usual field emission type magnetron.
  • a cathode part 5 is disposed in a central part of a plurality of anode vanes 1 .
  • the cathode part 5 has a structure that a plurality of field emission electrodes 6 made of metallic thin films formed in disk shapes with edges sharpened by an electric corrosive method are combined with a plurality of cathode substrates 8 to which oxide films 7 are applied to have a high secondary electron gain and the combined members are held between end hats 9 .
  • the oxide films 7 of the cathode substrates 8 are arranged to emit many secondary electrons when electrons from the field emission electrodes 6 rush.
  • thermo-electron emission type magnetron since the temperature of the cathode reaches about 2000K, an expensive material having a high melting point has needed to be used in the periphery of the cathode.
  • thermoelectron emission type magnetron In the usual thermoelectron emission type magnetron, a heater power source for heating the cathode has been separately necessary as well as a high voltage power source for applying voltage between the anode and the cathode of the magnetron.
  • thermoelectron emission type magnetron undesirably has a problem that it takes time to supply electric current to the cathode and obtain a desired operating temperature.
  • thermoelectron emission type magnetron inconveniently needs to raise the temperature of the cathode and the cathode undesirably consumes electric power.
  • An object of the present invention is to provide a magnetron having a cathode part whose life can be lengthened with a simple structure.
  • a magnetron according to the present invention has an anode part and a cathode part disposed coaxially.
  • Graphite nano-fibers are arranged on the electron emission surface of the cathode part.
  • the cathode part is provided with an oxide material film high in its secondary electron gain arranged in a part of the electron emission surface.
  • the cathode part is preferably formed in the form of a circular post or in a cylindrical shape.
  • the cathode part is preferably formed in the shape of a polygonal post or in a polygonal tubular shape.
  • the mixture of oxide whose particle diameter is several microns to several ten microns and graphite nano-fibers as a powdered material is applied on the surface of a cathode substrate to obtain an electron emission source.
  • a part of the electron emission source is preferably formed with filaments.
  • the graphite nano-fibers or carbon fibers are used for the cathode part so that the operating temperature of the cathode is lowered.
  • the peripheral part of the cathode can be formed with inexpensive metal such as stainless steel.
  • the graphite nano-fibers or carbon fibers are used for the cathode part so that a power source for heating the cathode is not required.
  • a power source for the magnetron or the structure of the magnetron can be greatly simplified.
  • the graphite nano-fibers or carbon fibers are used for the cathode part so that the magnetron can perform an instantaneous operation after voltage is applied to the magnetron.
  • the graphite nano-fibers or carbon fibers are used for the cathode part so that the consumed electric power of the cathode becomes zero. Thus, energy can be greatly saved.
  • the graphite nano-fibers or carbon fibers are used for the cathode part so that a mass-production can be achieved in a stable manner by using various kinds of CVD methods.
  • the graphite nano-fibers or carbon fibers are used for the cathode part so that electron can be uniformly emitted from the entire part of a film. Thus, the life of the magnetron is lengthened.
  • FIG. 1 is a longitudinally sectional view showing the structure of main parts of a magnetron having a cathode part with graphite nano-fibers formed on the surface of the cathode in a first embodiment of the present invention.
  • FIG. 2 is a longitudinally sectional view of a magnetron having a cold cathode in which graphite nano-fibers are used for a primary electron emission source and an oxide material film is used for a secondary electron emission source in a second embodiment of the present invention.
  • FIG. 3 is an axially vertical sectional view of a magnetron having a cathode in which graphite nano-fibers are allowed to grow on a flat plate and the plurality of the flat plates are arranged so as to have a polygonal post in a third embodiment of the present invention.
  • FIG. 4 is an enlarged schematic view of the surface of a cathode having a cold cathode in which powdered graphite nano-fibers and oxide slurry are applied to the surface of the cathode in a fourth embodiment of the present invention.
  • FIG. 5 is a longitudinally sectional view showing the structure of main parts of a magnetron having a cathode using graphite nano-fibers and filaments in a fifth embodiment of the present invention.
  • FIG. 6 is a longitudinally sectional view showing the structure of main parts of a usual thermoelectron emission type magnetron.
  • FIG. 7 is a longitudinally sectional view showing the structure of main parts of a usual field emission type magnetron.
  • FIG. 1 is a longitudinally sectional view showing the structure of main parts of a magnetron having a cathode part with graphite nano-fibers formed on the surface of the cathode in a first embodiment of the present invention.
  • a cathode substrate 10 is heated to 400 to 600° C. in the atmosphere of hydrocarbon gas such as methane and the gas is allowed to react with the surface of the cathode substrate 10 by a thermal CVD method.
  • hydrocarbon gas such as methane
  • an electron emission source in which graphite nano-fibers 11 are allowed to grow in a gaseous-phase on the surface of the cathode substrate 10 by using nickel or iron existing on the surface of the cathode substrate 10 as a nucleus is held between upper and lower end hats 12 to form a cylindrical cathode part 13 .
  • the graphite nano-fibers are employed as the electron emission source, so that a field concentration effect can be improved owing to the form thereof. Accordingly, ordinarily used voltage (several kV to several ten kV) is applied to the surface of the cathode part to easily obtain a strong electric filed (10 9 V/m). Thus, a potential barrier on the surface of the cathode becomes thin to generate a tunnel effect due to the surge characteristics of electrons and emit the electrons to a space without heating.
  • FIG. 2 is a longitudinally sectional view showing the structure of main parts of a cold cathode magnetron according to a second embodiment of the present invention.
  • graphite nano-fibers are employed as a primary electron emission source and an oxide material film is used as a secondary electron emission source.
  • barium carbonate is deposited on the outer peripheral surface of a cylindrical cathode substrate 16 by a thermal CVD method. Then, barium carbonate on the outer peripheral surface of the cathode substrate 16 is heated at 800° C. in vacuum and thermally decomposed to barium oxide.
  • secondary electron emission sources having oxide material films 17 formed are arranged at both ends in the axial direction of a primary electron emission source made of a cylindrical cathode substrate 10 on which graphite nano-fibers 11 are formed.
  • the barium oxide film advantageously has a secondary electron emission ratio as high as 4.8 among the oxide material films.
  • Strontium oxide or calcium oxide may be used.
  • a split anode is an anode for an existing magnetron (divided into ten, inside diameter of 8 mm).
  • the above-described cathode part was arranged coaxially with the anode to assemble a magnetron vacuum tube.
  • a pair of magnets (not shown in the drawing) were axially disposed.
  • a direct current magnetic field 18 was generated for 0.35 T
  • voltage of ⁇ 6.0 kV was applied to the cathode part 10 .
  • a radial electric field 19 generated due to voltage between the anode and the cathode caused a field emission phenomenon to be generated in the graphite nano-fibers 11 of the cathode part 15 and electrons to be emitted.
  • the thickness of the graphite nano-fibers was not uniform. Accordingly, protruding graphite nano-fibers abnormally discharged. In this case, the protruding parts were eliminated due to the discharge. After the abnormal discharges of several times, emission parts were distributed. Finally, substantially all the surface of the graphite nano-fiber film uniformly emitted the electrons.
  • the electrons made a cyclotron motion by the axial direct current magnetic field 18 and rushed to the oxide material films 17 .
  • an electric current of 60 mA was maximally supplied between the anode and the cathode and an oscillation of 250 W was maximally obtained under 2.45 GHz.
  • FIG. 3 is an axially vertical sectional view showing the structure of main parts of a magnetron according to a third embodiment of the present invention in which graphite nano-fibers are allowed to grow on a plate shaped cathode substrate and a plurality of the cathode substrates are arranged so as to form a polygonal post as a cathode part.
  • the cathode part 20 of the magnetron is formed in such a manner that the graphite nano-fibers 11 are allowed to grow on the plate shaped cathode substrate 21 to combine the cathode substrates into an octagonal post and obtain a cathode part. Since the cathode substrate 21 is plate shaped, the graphite nano-fibers 11 are preferably easily formed on the surface of the cathode substrate 21 .
  • FIG. 4 is an enlarged schematic view of the cathode surface of a cold cathode formed by applying powdered graphite nano-fibers and oxide slurry on the surface of the cathode in a fourth embodiment of the present invention.
  • the mixture of slurry obtained by mixing carbonate whose particle diameter is several microns to several ten microns with a binder and powdered graphite nano-fibers is applied to the surface of a cathode substrate 22 and heated to change the carbonate to oxides 23 .
  • the graphite nano-fibers 11 are used for an electron emission source for emitting primary electrons.
  • the oxides 23 on the surface of the cathode are used as an electron emission source for emitting secondary electrons.
  • an electric field does not focus, so that the cathode substrate is not used for a field emission electrode.
  • the particles of the carbonate support the graphite nano-fibers, so that the graphite nano-fibers can be vertically fixed to the cathode substrate.
  • an electrode film can be easily formed only by applying the mixture to the cathode substrate.
  • FIG. 5 is a longitudinally sectional view showing the structure of main parts of a magnetron according to a fifth embodiment of the present invention in which a cathode using graphite nano-fibers and filaments is provided.
  • a cathode part 24 of the magnetron is formed with filaments 25 partly made of thorium tungsten and a part of end hats 26 for holding the filaments 25 between them is formed with the graphite nano-fibers 11 .
  • the initial operation of the magnetron is carried out by electrons emitted from the graphite nano-fibers 11 .
  • thermoelectrons are emitted from the filaments 25 .
  • a larger quantity of electric current can be obtained between an anode and the cathode upon operation of the magnetron.
  • the present invention can be used for a high frequency heating device such as a microwave range, radar, air-crafts, marine vessels, space-crafts, rockets, etc.

Abstract

A cathode substrate 10 is heated to 400 to 600° C. in the atmosphere of hydrocarbon gas such as methane and the gas is allowed to react with the surface of the cathode substrate 10 by a thermal CVD method. Thus, an electron emission source in which graphite nano-fibers 11 are allowed to grow in a gaseous-phase on the surface of the cathode substrate 10 by using nickel or iron existing on the surface of the cathode substrate 10 as a nucleus is held between upper and lower end hats 12 to form a cathode part 13.

Description

    BACKGROUND OF THE INVENTION
  • The present invention relates to a field emission type magnetron used for a high frequency heating device such as a microwave range or a pulse generator such as a radar.
  • In a usual thermo-electron emission type magnetron, a hot cathode is used as an electron source. The hot cathode supplies electrons by emitting thermo-electrons. A thermo-electron emission is a mechanism that free electrons of a conduction band of the cathode obtain thermal energy by heating a material at about 1500 to 2700 K so that the free electrons get over a surface potential barrier to be emitted to a space.
  • FIG. 6 is a longitudinally sectional view showing one example of a usual thermo-electron emission type magnetron. In the drawing, a hot cathode 2 is disposed at a central part of a plurality of anode vanes 1. The hot cathode 2 is formed in such a manner that tungsten wire rods 3 including thorium are formed helically at substantially equal intervals and both end parts are held by end hat parts 4. Electric current is supplied to the hot cathode 2 to raise the temperature of the cathode to about 2000K and emit thermo-electrons (for instance, see JP-A-2001-23531).
  • Further, a field emission type magnetron provided with a cathode that employs a usual field emission phenomenon uses a metallic foil as an electrode, as well known (for instance, see Japanese Patent No.2740793).
  • The field emission phenomenon means a phenomenon that a high electric field (about 109 V/m) is applied to a part near the surface of a material to allow the potential barrier on the surface of the material to be thin and electrons to be emitted outside the material without getting over the potential barrier due to a tunnel effect generated by the surge characteristics of the electrons. In the case of the magnetron of a cm band in which the voltage of the cathode is located within a range of several kV to several ten kV, the field intensity of the surface of the cathode is 107 V/m. Thus, when the electric field is not intensified approximately by two digits, the field emission is not generated. Accordingly, in order to realize the field emission in the cathode for the magnetron, an electrode for a field emission needs to have a structure that a radius of curvature of an end is small like a needle or a foil and improve a field concentration effect.
  • FIG. 7 is a longitudinally sectional view showing the structure of main parts of the usual field emission type magnetron. In the drawing, a cathode part 5 is disposed in a central part of a plurality of anode vanes 1. The cathode part 5 has a structure that a plurality of field emission electrodes 6 made of metallic thin films formed in disk shapes with edges sharpened by an electric corrosive method are combined with a plurality of cathode substrates 8 to which oxide films 7 are applied to have a high secondary electron gain and the combined members are held between end hats 9. The oxide films 7 of the cathode substrates 8 are arranged to emit many secondary electrons when electrons from the field emission electrodes 6 rush.
  • In the usual thermo-electron emission type magnetron, since the temperature of the cathode reaches about 2000K, an expensive material having a high melting point has needed to be used in the periphery of the cathode.
  • In the usual thermoelectron emission type magnetron, a heater power source for heating the cathode has been separately necessary as well as a high voltage power source for applying voltage between the anode and the cathode of the magnetron.
  • The usual thermoelectron emission type magnetron undesirably has a problem that it takes time to supply electric current to the cathode and obtain a desired operating temperature.
  • Further, the usual thermoelectron emission type magnetron inconveniently needs to raise the temperature of the cathode and the cathode undesirably consumes electric power.
  • Further, in the usual field emission type magnetron, a work for sharpening the edges of metallic foils as field emission electrodes has been difficult. Further, a stable production has been difficult.
  • Since field intensities applied to a plurality of field emission electrodes are respectively different, electric currents emitted from the electrodes are not respectively uniform. Therefore, the electrode to which a load is applied is especially seriously exhausted, so that the function of the electrode is firstly deteriorated. This phenomenon undesirably causes the life of the whole of the cathode to be shortened.
  • Since a large number of field emission electrodes as primary electron emission sources and electrodes as secondary electron emission sources for multiplying electrons emitted from an electric field needs to be coaxially arranged, the number of parts is undesirably large, an assembly thereof is difficult and a cost is high.
  • SUMMARY OF THE INVENTION
  • An object of the present invention is to provide a magnetron having a cathode part whose life can be lengthened with a simple structure.
  • In order to solve the above-described problems, a magnetron according to the present invention has an anode part and a cathode part disposed coaxially. Graphite nano-fibers are arranged on the electron emission surface of the cathode part.
  • The cathode part is provided with an oxide material film high in its secondary electron gain arranged in a part of the electron emission surface.
  • Further, the cathode part is preferably formed in the form of a circular post or in a cylindrical shape.
  • Further, the cathode part is preferably formed in the shape of a polygonal post or in a polygonal tubular shape.
  • In another magnetron according to the present invention, the mixture of oxide whose particle diameter is several microns to several ten microns and graphite nano-fibers as a powdered material is applied on the surface of a cathode substrate to obtain an electron emission source.
  • Further, a part of the electron emission source is preferably formed with filaments.
  • According to the present invention, such advantages as described below are realized.
  • The graphite nano-fibers or carbon fibers are used for the cathode part so that the operating temperature of the cathode is lowered. Thus, the peripheral part of the cathode can be formed with inexpensive metal such as stainless steel.
  • The graphite nano-fibers or carbon fibers are used for the cathode part so that a power source for heating the cathode is not required. Thus, a power source for the magnetron or the structure of the magnetron can be greatly simplified.
  • The graphite nano-fibers or carbon fibers are used for the cathode part so that the magnetron can perform an instantaneous operation after voltage is applied to the magnetron.
  • The graphite nano-fibers or carbon fibers are used for the cathode part so that the consumed electric power of the cathode becomes zero. Thus, energy can be greatly saved.
  • The graphite nano-fibers or carbon fibers are used for the cathode part so that a mass-production can be achieved in a stable manner by using various kinds of CVD methods.
  • The graphite nano-fibers or carbon fibers are used for the cathode part so that electron can be uniformly emitted from the entire part of a film. Thus, the life of the magnetron is lengthened.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a longitudinally sectional view showing the structure of main parts of a magnetron having a cathode part with graphite nano-fibers formed on the surface of the cathode in a first embodiment of the present invention.
  • FIG. 2 is a longitudinally sectional view of a magnetron having a cold cathode in which graphite nano-fibers are used for a primary electron emission source and an oxide material film is used for a secondary electron emission source in a second embodiment of the present invention.
  • FIG. 3 is an axially vertical sectional view of a magnetron having a cathode in which graphite nano-fibers are allowed to grow on a flat plate and the plurality of the flat plates are arranged so as to have a polygonal post in a third embodiment of the present invention.
  • FIG. 4 is an enlarged schematic view of the surface of a cathode having a cold cathode in which powdered graphite nano-fibers and oxide slurry are applied to the surface of the cathode in a fourth embodiment of the present invention.
  • FIG. 5 is a longitudinally sectional view showing the structure of main parts of a magnetron having a cathode using graphite nano-fibers and filaments in a fifth embodiment of the present invention.
  • FIG. 6 is a longitudinally sectional view showing the structure of main parts of a usual thermoelectron emission type magnetron.
  • FIG. 7 is a longitudinally sectional view showing the structure of main parts of a usual field emission type magnetron.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Now, an embodiment of a magnetron according to the present invention will be described by referring to the drawings.
  • (First Embodiment)
  • FIG. 1 is a longitudinally sectional view showing the structure of main parts of a magnetron having a cathode part with graphite nano-fibers formed on the surface of the cathode in a first embodiment of the present invention.
  • In this embodiment, a cathode substrate 10 is heated to 400 to 600° C. in the atmosphere of hydrocarbon gas such as methane and the gas is allowed to react with the surface of the cathode substrate 10 by a thermal CVD method. Thus, an electron emission source in which graphite nano-fibers 11 are allowed to grow in a gaseous-phase on the surface of the cathode substrate 10 by using nickel or iron existing on the surface of the cathode substrate 10 as a nucleus is held between upper and lower end hats 12 to form a cylindrical cathode part 13.
  • Since a current path for heating the cathode is not necessary, one connecting terminal 14 is required as compared with two usual hot cathodes as shown in FIG. 6.
  • The graphite nano-fibers are employed as the electron emission source, so that a field concentration effect can be improved owing to the form thereof. Accordingly, ordinarily used voltage (several kV to several ten kV) is applied to the surface of the cathode part to easily obtain a strong electric filed (109 V/m). Thus, a potential barrier on the surface of the cathode becomes thin to generate a tunnel effect due to the surge characteristics of electrons and emit the electrons to a space without heating.
  • (Second Embodiment)
  • FIG. 2 is a longitudinally sectional view showing the structure of main parts of a cold cathode magnetron according to a second embodiment of the present invention. In the second embodiment, graphite nano-fibers are employed as a primary electron emission source and an oxide material film is used as a secondary electron emission source.
  • According to this embodiment, in a cathode part 15 of the magnetron, barium carbonate is deposited on the outer peripheral surface of a cylindrical cathode substrate 16 by a thermal CVD method. Then, barium carbonate on the outer peripheral surface of the cathode substrate 16 is heated at 800° C. in vacuum and thermally decomposed to barium oxide. Thus, secondary electron emission sources having oxide material films 17 formed are arranged at both ends in the axial direction of a primary electron emission source made of a cylindrical cathode substrate 10 on which graphite nano-fibers 11 are formed. The barium oxide film advantageously has a secondary electron emission ratio as high as 4.8 among the oxide material films. Strontium oxide or calcium oxide may be used.
  • A split anode is an anode for an existing magnetron (divided into ten, inside diameter of 8 mm). The above-described cathode part was arranged coaxially with the anode to assemble a magnetron vacuum tube. A pair of magnets (not shown in the drawing) were axially disposed. Thus, while a direct current magnetic field 18 was generated for 0.35 T, voltage of −6.0 kV was applied to the cathode part 10. A radial electric field 19 generated due to voltage between the anode and the cathode caused a field emission phenomenon to be generated in the graphite nano-fibers 11 of the cathode part 15 and electrons to be emitted. When the voltage was firstly applied to the cathode part, the thickness of the graphite nano-fibers was not uniform. Accordingly, protruding graphite nano-fibers abnormally discharged. In this case, the protruding parts were eliminated due to the discharge. After the abnormal discharges of several times, emission parts were distributed. Finally, substantially all the surface of the graphite nano-fiber film uniformly emitted the electrons.
  • The electrons made a cyclotron motion by the axial direct current magnetic field 18 and rushed to the oxide material films 17. Thus, many secondary electrons were emitted, an electric current of 60 mA was maximally supplied between the anode and the cathode and an oscillation of 250 W was maximally obtained under 2.45 GHz.
  • (Third Embodiment)
  • FIG. 3 is an axially vertical sectional view showing the structure of main parts of a magnetron according to a third embodiment of the present invention in which graphite nano-fibers are allowed to grow on a plate shaped cathode substrate and a plurality of the cathode substrates are arranged so as to form a polygonal post as a cathode part.
  • According to this embodiment, the cathode part 20 of the magnetron is formed in such a manner that the graphite nano-fibers 11 are allowed to grow on the plate shaped cathode substrate 21 to combine the cathode substrates into an octagonal post and obtain a cathode part. Since the cathode substrate 21 is plate shaped, the graphite nano-fibers 11 are preferably easily formed on the surface of the cathode substrate 21.
  • (Fourth Embodiment)
  • FIG. 4 is an enlarged schematic view of the cathode surface of a cold cathode formed by applying powdered graphite nano-fibers and oxide slurry on the surface of the cathode in a fourth embodiment of the present invention.
  • According to this embodiment, in the cathode part of the magnetron, the mixture of slurry obtained by mixing carbonate whose particle diameter is several microns to several ten microns with a binder and powdered graphite nano-fibers is applied to the surface of a cathode substrate 22 and heated to change the carbonate to oxides 23. The graphite nano-fibers 11 are used for an electron emission source for emitting primary electrons. The oxides 23 on the surface of the cathode are used as an electron emission source for emitting secondary electrons. When only the graphite nano-fibers are applied on the cathode substrate, the graphite nano-fibers are laid and fixed onto the cathode substrate. Thus, an electric field does not focus, so that the cathode substrate is not used for a field emission electrode. However, when particulate carbonate is used, the particles of the carbonate support the graphite nano-fibers, so that the graphite nano-fibers can be vertically fixed to the cathode substrate. Thus, in this structure, an electrode film can be easily formed only by applying the mixture to the cathode substrate.
  • (Fifth Embodiment)
  • FIG. 5 is a longitudinally sectional view showing the structure of main parts of a magnetron according to a fifth embodiment of the present invention in which a cathode using graphite nano-fibers and filaments is provided.
  • In this embodiment, a cathode part 24 of the magnetron is formed with filaments 25 partly made of thorium tungsten and a part of end hats 26 for holding the filaments 25 between them is formed with the graphite nano-fibers 11. In this structure, the initial operation of the magnetron is carried out by electrons emitted from the graphite nano-fibers 11. After that, when the temperature of the cathode part 24 rises by energy when the electrons rush again into the cathode, thermoelectrons are emitted from the filaments 25. Thus, a larger quantity of electric current can be obtained between an anode and the cathode upon operation of the magnetron.
  • The present invention can be used for a high frequency heating device such as a microwave range, radar, air-crafts, marine vessels, space-crafts, rockets, etc.

Claims (7)

1. A magnetron comprising:
an anode part;
a cathode part disposed coaxially with said anode part, having an electron emission surface; and
graphite nano-fibers arranged on the electron emission surface of the cathode part.
2. A magnetron according to claim 1, wherein the cathode part includes an oxide material film high in its secondary electron gain arranged in a part of the electron emission surface.
3. A magnetron according to claims 1 to 2, wherein the cathode part is formed in the form of a circular post or in a cylindrical shape.
4. A magnetron according to claims 1 to 2, wherein the cathode part is formed in the shape of a polygonal post or in a polygonal tubular shape.
5. A magnetron according to claim 2, wherein the mixture of oxide whose particle diameter is several microns to several ten microns and graphite nano-fibers as a powdered material is applied on the surface of a cathode substrate to obtain an electron emission source.
6. A magnetron according to claim 2, wherein a part of the electron emission source is formed with filaments.
7. A magnetron according to claims 1 or 2, wherein one connecting terminal from the cathode is used.
US10/912,099 2003-08-07 2004-08-06 Magnetron with graphite nano-fibers on cathode Expired - Fee Related US7474042B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JPP.2003-288752 2003-08-07
JP2003288752A JP2005056785A (en) 2003-08-07 2003-08-07 Magnetron

Publications (2)

Publication Number Publication Date
US20050029917A1 true US20050029917A1 (en) 2005-02-10
US7474042B2 US7474042B2 (en) 2009-01-06

Family

ID=33550047

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/912,099 Expired - Fee Related US7474042B2 (en) 2003-08-07 2004-08-06 Magnetron with graphite nano-fibers on cathode

Country Status (6)

Country Link
US (1) US7474042B2 (en)
EP (1) EP1505627B1 (en)
JP (1) JP2005056785A (en)
KR (1) KR101100919B1 (en)
CN (1) CN1581410A (en)
DE (1) DE602004023567D1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110186735A1 (en) * 2010-02-04 2011-08-04 Hitachi, Ltd. Electron source, electron gun, and electron microscope device and electron beam lithography device using it
CN105355525A (en) * 2015-12-03 2016-02-24 中国人民解放军国防科学技术大学 Fiber array cathode
RU168920U1 (en) * 2016-08-25 2017-02-28 Акционерное общество "Центр Фундаментальных и прикладных исследований РАН" MAGNETRON

Families Citing this family (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5074666B2 (en) * 2005-03-09 2012-11-14 パナソニック株式会社 Magnetron
JP4876471B2 (en) * 2005-08-02 2012-02-15 パナソニック株式会社 Field electron emission source and magnetron and microwave application apparatus using the same
RU2494489C1 (en) * 2012-02-10 2013-09-27 Общество с ограниченной ответственностью "Плутон Инвест" Magnetron with selfheated startup with special activation of field-emission cathodes
US20160216304A1 (en) 2015-01-28 2016-07-28 Lockheed Martin Corporation Rapid high-resolution magnetic field measurements for power line inspection
US9824597B2 (en) 2015-01-28 2017-11-21 Lockheed Martin Corporation Magnetic navigation methods and systems utilizing power grid and communication network
US9910104B2 (en) 2015-01-23 2018-03-06 Lockheed Martin Corporation DNV magnetic field detector
US10168393B2 (en) 2014-09-25 2019-01-01 Lockheed Martin Corporation Micro-vacancy center device
US9853837B2 (en) 2014-04-07 2017-12-26 Lockheed Martin Corporation High bit-rate magnetic communication
US9557391B2 (en) 2015-01-23 2017-01-31 Lockheed Martin Corporation Apparatus and method for high sensitivity magnetometry measurement and signal processing in a magnetic detection system
US9910105B2 (en) 2014-03-20 2018-03-06 Lockheed Martin Corporation DNV magnetic field detector
US9614589B1 (en) 2015-12-01 2017-04-04 Lockheed Martin Corporation Communication via a magnio
US10338162B2 (en) 2016-01-21 2019-07-02 Lockheed Martin Corporation AC vector magnetic anomaly detection with diamond nitrogen vacancies
US9638821B2 (en) 2014-03-20 2017-05-02 Lockheed Martin Corporation Mapping and monitoring of hydraulic fractures using vector magnetometers
GB2540308B (en) 2014-04-07 2018-05-16 Lockheed Corp Energy efficient controlled magnetic field generator circuit
WO2016126436A1 (en) 2015-02-04 2016-08-11 Lockheed Martin Corporation Apparatus and method for recovery of three dimensional magnetic field from a magnetic detection system
GB2550809A (en) 2015-02-04 2017-11-29 Lockheed Corp Apparatus and method for estimating absolute axes' orientations for a magnetic detection system
CN105118764B (en) * 2015-07-18 2017-09-19 中国人民解放军国防科学技术大学 A kind of disk array cathode
EP3371614A1 (en) 2015-11-04 2018-09-12 Lockheed Martin Corporation Magnetic band-pass filter
WO2017087013A1 (en) 2015-11-20 2017-05-26 Lockheed Martin Corporation Apparatus and method for closed loop processing for a magnetic detection system
WO2017087014A1 (en) 2015-11-20 2017-05-26 Lockheed Martin Corporation Apparatus and method for hypersensitivity detection of magnetic field
WO2017123261A1 (en) 2016-01-12 2017-07-20 Lockheed Martin Corporation Defect detector for conductive materials
EP3405603A4 (en) 2016-01-21 2019-10-16 Lockheed Martin Corporation Diamond nitrogen vacancy sensor with circuitry on diamond
WO2017127096A1 (en) 2016-01-21 2017-07-27 Lockheed Martin Corporation Diamond nitrogen vacancy sensor with dual rf sources
WO2017127090A1 (en) 2016-01-21 2017-07-27 Lockheed Martin Corporation Higher magnetic sensitivity through fluorescence manipulation by phonon spectrum control
WO2017127098A1 (en) 2016-01-21 2017-07-27 Lockheed Martin Corporation Diamond nitrogen vacancy sensed ferro-fluid hydrophone
WO2017127097A1 (en) 2016-01-21 2017-07-27 Lockheed Martin Corporation Magnetometer with a light emitting diode
GB2562193B (en) 2016-01-21 2021-12-22 Lockheed Corp Diamond nitrogen vacancy sensor with common RF and magnetic fields generator
WO2017127094A1 (en) 2016-01-21 2017-07-27 Lockheed Martin Corporation Magnetometer with light pipe
CN105810536B (en) * 2016-03-31 2018-01-12 电子科技大学 Using the magnetron of combined type cold cathode head and the production method of cold cathode body
US10345395B2 (en) 2016-12-12 2019-07-09 Lockheed Martin Corporation Vector magnetometry localization of subsurface liquids
US10677953B2 (en) 2016-05-31 2020-06-09 Lockheed Martin Corporation Magneto-optical detecting apparatus and methods
US10345396B2 (en) 2016-05-31 2019-07-09 Lockheed Martin Corporation Selected volume continuous illumination magnetometer
US10408890B2 (en) 2017-03-24 2019-09-10 Lockheed Martin Corporation Pulsed RF methods for optimization of CW measurements
US10145910B2 (en) 2017-03-24 2018-12-04 Lockheed Martin Corporation Photodetector circuit saturation mitigation for magneto-optical high intensity pulses
US20170343621A1 (en) 2016-05-31 2017-11-30 Lockheed Martin Corporation Magneto-optical defect center magnetometer
US10274550B2 (en) 2017-03-24 2019-04-30 Lockheed Martin Corporation High speed sequential cancellation for pulsed mode
US10281550B2 (en) 2016-11-14 2019-05-07 Lockheed Martin Corporation Spin relaxometry based molecular sequencing
US10571530B2 (en) 2016-05-31 2020-02-25 Lockheed Martin Corporation Buoy array of magnetometers
US10338163B2 (en) 2016-07-11 2019-07-02 Lockheed Martin Corporation Multi-frequency excitation schemes for high sensitivity magnetometry measurement with drift error compensation
US10228429B2 (en) 2017-03-24 2019-03-12 Lockheed Martin Corporation Apparatus and method for resonance magneto-optical defect center material pulsed mode referencing
US10527746B2 (en) 2016-05-31 2020-01-07 Lockheed Martin Corporation Array of UAVS with magnetometers
US10317279B2 (en) 2016-05-31 2019-06-11 Lockheed Martin Corporation Optical filtration system for diamond material with nitrogen vacancy centers
US10330744B2 (en) 2017-03-24 2019-06-25 Lockheed Martin Corporation Magnetometer with a waveguide
US10371765B2 (en) 2016-07-11 2019-08-06 Lockheed Martin Corporation Geolocation of magnetic sources using vector magnetometer sensors
US10359479B2 (en) 2017-02-20 2019-07-23 Lockheed Martin Corporation Efficient thermal drift compensation in DNV vector magnetometry
US10371760B2 (en) 2017-03-24 2019-08-06 Lockheed Martin Corporation Standing-wave radio frequency exciter
US10338164B2 (en) 2017-03-24 2019-07-02 Lockheed Martin Corporation Vacancy center material with highly efficient RF excitation
US10459041B2 (en) 2017-03-24 2019-10-29 Lockheed Martin Corporation Magnetic detection system with highly integrated diamond nitrogen vacancy sensor
US10379174B2 (en) 2017-03-24 2019-08-13 Lockheed Martin Corporation Bias magnet array for magnetometer
CN109830416A (en) * 2019-02-22 2019-05-31 长沙魔豆智能科技有限公司 A kind of electron emitter and magnetron
CN111120234B (en) * 2019-12-19 2021-02-23 上海航天控制技术研究所 Graphite high-temperature cathode device for electric thruster
CN113097032B (en) * 2021-04-23 2023-10-20 西北核技术研究所 Long-life micro-column array graphite and metal composite cathode structure and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2803773A (en) * 1952-10-28 1957-08-20 Gen Electric High frequency diode magnetron
US5317006A (en) * 1989-06-15 1994-05-31 Microelectronics And Computer Technology Corporation Cylindrical magnetron sputtering system
US20020060516A1 (en) * 2000-09-01 2002-05-23 Shinichi Kawate Electron-emitting devices, electron sources, and image-forming apparatus
US20020125827A1 (en) * 2001-03-08 2002-09-12 Genvac Aerospace Corporation Magnetron with diamond coated cathode
US6717340B2 (en) * 2001-09-26 2004-04-06 Canon Kabushiki Kaisha Electron-emitting device and image-forming apparatus

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52102667A (en) 1976-02-24 1977-08-29 Japan Radio Co Ltd Structure of magnetron cathode
RU2007777C1 (en) 1992-04-15 1994-02-15 Предприятие "Плутон" Magnetron
JP2000100339A (en) 1998-09-25 2000-04-07 Sharp Corp Magnetron
JP2001023531A (en) 1999-07-09 2001-01-26 Hitachi Ltd Magnetron
JP3481578B2 (en) 1999-10-12 2003-12-22 松下電器産業株式会社 Electron-emitting device, electron source using the same, field-emission-type image display device, fluorescent lamp, and manufacturing method thereof
TW494423B (en) 1999-10-12 2002-07-11 Matsushita Electric Ind Co Ltd Elecron-emitting element, electronic source using the element, field emission display device, fluorescent lamp, and method for producing those
US6724146B2 (en) 2001-11-27 2004-04-20 Raytheon Company Phased array source of electromagnetic radiation
US6373194B1 (en) * 2000-06-01 2002-04-16 Raytheon Company Optical magnetron for high efficiency production of optical radiation
JP2003242898A (en) 2002-02-19 2003-08-29 Matsushita Electric Ind Co Ltd Magnetron

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2803773A (en) * 1952-10-28 1957-08-20 Gen Electric High frequency diode magnetron
US5317006A (en) * 1989-06-15 1994-05-31 Microelectronics And Computer Technology Corporation Cylindrical magnetron sputtering system
US20020060516A1 (en) * 2000-09-01 2002-05-23 Shinichi Kawate Electron-emitting devices, electron sources, and image-forming apparatus
US20020125827A1 (en) * 2001-03-08 2002-09-12 Genvac Aerospace Corporation Magnetron with diamond coated cathode
US6717340B2 (en) * 2001-09-26 2004-04-06 Canon Kabushiki Kaisha Electron-emitting device and image-forming apparatus

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110186735A1 (en) * 2010-02-04 2011-08-04 Hitachi, Ltd. Electron source, electron gun, and electron microscope device and electron beam lithography device using it
CN105355525A (en) * 2015-12-03 2016-02-24 中国人民解放军国防科学技术大学 Fiber array cathode
RU168920U1 (en) * 2016-08-25 2017-02-28 Акционерное общество "Центр Фундаментальных и прикладных исследований РАН" MAGNETRON

Also Published As

Publication number Publication date
EP1505627A3 (en) 2008-03-05
CN1581410A (en) 2005-02-16
EP1505627A2 (en) 2005-02-09
JP2005056785A (en) 2005-03-03
US7474042B2 (en) 2009-01-06
KR20050016209A (en) 2005-02-21
EP1505627B1 (en) 2009-10-14
KR101100919B1 (en) 2012-01-02
DE602004023567D1 (en) 2009-11-26

Similar Documents

Publication Publication Date Title
US7474042B2 (en) Magnetron with graphite nano-fibers on cathode
KR0176876B1 (en) Magnetron
US3374386A (en) Field emission cathode having tungsten miller indices 100 plane coated with zirconium, hafnium or magnesium on oxygen binder
US7129708B1 (en) Vacuum ionization gauge with high sensitivity
US6359378B1 (en) Amplifier having multilayer carbon-based field emission cathode
US8253314B2 (en) Ion source having secondary electron enhancing electrode
US20030143356A1 (en) Carbon nanotube for electron emission source and manufacturing method therefor
JP4849576B2 (en) Cathode body and fluorescent tube using the same
US20080267354A1 (en) High-Dose X-Ray Tube
US6441550B1 (en) Carbon-based field emission electron device for high current density applications
US8237347B2 (en) Field emission device having secondary electron enhancing electrode
US2399003A (en) Electric discharge device
JP2003242898A (en) Magnetron
US2683237A (en) Radio frequency tube with low internal impedance
US8246413B2 (en) Method for making field emission device
Egorov et al. Field emission cathode-based devices and equipment
Kuznetsov Cathodes for electron guns
US3555334A (en) Cathode with graphite end shields
CN110379690B (en) Cold cathode electron gun using radio frequency excitation field to emit electron beam
US2430482A (en) Gaseous electric lamp
US1971812A (en) X-ray device
JP2004241352A (en) Cathode for magnetron, and magnetron using the same
KR100343557B1 (en) Electric-gun using arbon nano tube field emission degauss
RU2528982C2 (en) Magnetron having triggering emitters at end shields of cathode assemblies
CN111554558A (en) Field emission cold cathode soft X-ray tube using carbon nano tube

Legal Events

Date Code Title Description
AS Assignment

Owner name: MATSUSHITA ELECTRIC INDUSTRIAL CO. LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:AIGA, MASAYUKI;TSUKADA, TOSHIYUKI;REEL/FRAME:015668/0107

Effective date: 20040730

AS Assignment

Owner name: PANASONIC CORPORATION, JAPAN

Free format text: CHANGE OF NAME;ASSIGNOR:MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD.;REEL/FRAME:021832/0215

Effective date: 20081001

Owner name: PANASONIC CORPORATION,JAPAN

Free format text: CHANGE OF NAME;ASSIGNOR:MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD.;REEL/FRAME:021832/0215

Effective date: 20081001

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20170106